FDA Drug Recalls

Recalls / Class II

Class IID-1067-2017

Product

Glycopyrrolate Injection Solution, 1 mL 0.2 mg/1 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-45

Affected lot / code info
Lot #: 9868, BUD: 8/9/2017; 9872, BUD: 8/10/2017; 10318, BUD: 10/7/2017

Why it was recalled

Lack of Sterility Assurance.

Recalling firm

Firm
Cantrell Drug Company
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
7321 Cantrell Rd, N/A, Little Rock, Arkansas 72207-4144

Distribution

Quantity
5245 syringes
Distribution pattern
Nationwide within the US

Timeline

Recall initiated
2017-07-14
FDA classified
2017-08-09
Posted by FDA
2017-08-16
Terminated
2020-09-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1067-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.